Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Å
±: %
SMI:

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_cd7595814d95f8dcea37e990e983cac3 Metamitron [M+H]+ 203.0927 0.78 141.71 CC1=NN=C(C(=O)N1N)C2=CC=CC=C2  Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_0e142ffe91e5387e2be29eee8a4f8729 Methabenzthiazuron [M+H]+ 222.0696 0.86 143.34 CNC(=O)N(C)C1=NC2=CC=CC=C2S1   Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_f47d04c7657c562edc46f0dd8f9da36a Methfuroxam [M+H]+ 230.1176 0.88 152.88 CC1=C(OC(=C1C(=O)NC2=CC=CC=C2)C)C   Benzenoids 1 1 TW polyala
CCSBASE_1f365b90cba5a59c1699155cdf6ae6b0 Methfuroxam [M+H-H2O]+ 212.1071 0.88 144.62 CC1=C(OC(=C1C(=O)NC2=CC=CC=C2)C)C   Benzenoids 1 1 TW polyala
CCSBASE_ea6c3a487a22d274d6a6bfc97b8f75e3 Methfuroxam [M+Na]+ 252.0995 0.88 165.46 CC1=C(OC(=C1C(=O)NC2=CC=CC=C2)C)C   Benzenoids 1 1 TW polyala
CCSBASE_b5a3f6b51173bc0aedf7ea5bc8255cf4 Methfuroxam [M-H]- 228.103 0.84 158.07 CC1=C(OC(=C1C(=O)NC2=CC=CC=C2)C)C Benzenoids -1 1 TW polyala
CCSBASE_854b03c38d78d5a8cb1d93f83b752803 Methylprednisolone [M+FA-H]- 419.2075 0.8 195.96 CC1CC2C3CCC(C3(CC(C2C4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_3a41a71584b546c7a76137a318d049db Methylprednisolone [M+H]+ 375.2166 0.86 187.1 C[C@H]1C[C@H]2[C@@H]3CC[C@@]([C@]3(C[C@@H]([C@@H]2[C@@]4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O   Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_a4d0cde286a681e2f70ba8a354059814 Methylprednisolone [M+H-H2O]+ 357.2061 0.86 185.02 C[C@H]1C[C@H]2[C@@H]3CC[C@@]([C@]3(C[C@@H]([C@@H]2[C@@]4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O   Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_95083252d8ddce2cbaaaf3e63aa7b805 Methylprednisolone [M+Na]+ 397.1985 0.86 210.23 C[C@H]1C[C@H]2[C@@H]3CC[C@@]([C@]3(C[C@@H]([C@@H]2[C@@]4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O   Lipids and lipid-like molecules 1 1 TW polyala
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